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INTERVIEW: MedTech Europe Ready To Guide Industry As MDR/IVDR Details Emerge

This article was originally published in SRA

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Executive Summary

Industry has long been holding its breath for an agreement to be reached on the new EU Medical Device and IVD Regulations. Now that the European Parliament and Council of the EU have finally agreed on the texts, the true enormity of the task ahead is unveiling itself. Amanda Maxwell spoke with MedTech Europe's John Brennan and Jesus Rueda to find out what lies ahead.

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This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

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